WO2003024976A3 - Tricyclic indole derivatives as 5-ht ligands - Google Patents

Tricyclic indole derivatives as 5-ht ligands Download PDF

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Publication number
WO2003024976A3
WO2003024976A3 PCT/US2002/030089 US0230089W WO03024976A3 WO 2003024976 A3 WO2003024976 A3 WO 2003024976A3 US 0230089 W US0230089 W US 0230089W WO 03024976 A3 WO03024976 A3 WO 03024976A3
Authority
WO
WIPO (PCT)
Prior art keywords
ligands
compounds
indole derivatives
tricyclic indole
formula
Prior art date
Application number
PCT/US2002/030089
Other languages
French (fr)
Other versions
WO2003024976A2 (en
Inventor
Jian-Min Fu
Original Assignee
Upjohn Co
Jian-Min Fu
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Upjohn Co, Jian-Min Fu filed Critical Upjohn Co
Priority to AU2002336749A priority Critical patent/AU2002336749A1/en
Priority to JP2003528823A priority patent/JP2005527477A/en
Priority to EP02773527A priority patent/EP1429776A2/en
Priority to MXPA04002615A priority patent/MXPA04002615A/en
Priority to CA002460126A priority patent/CA2460126A1/en
Priority to BRPI0212676-1A priority patent/BR0212676A/en
Publication of WO2003024976A2 publication Critical patent/WO2003024976A2/en
Publication of WO2003024976A3 publication Critical patent/WO2003024976A3/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/06—Peri-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Child & Adolescent Psychology (AREA)
  • Obesity (AREA)
  • Hospice & Palliative Care (AREA)
  • Anesthesiology (AREA)
  • Addiction (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

The present invention provides compounds of Formula (I) wherein: R1, R2, R3, R4, R5, R6, R7, R8, n, m, and X have any of the values defined in the specification, as well as pharmaceutical compositions comprising the compounds. The invention also provides therapeutic methods as well as processes and intermediates useful for preparing compounds of Formula (I). The compounds are 5-HT ligands and are useful for treating diseases wherein modulation of 5-HT activity is desired.
PCT/US2002/030089 2001-09-21 2002-09-19 Tricyclic indole derivatives as 5-ht ligands WO2003024976A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
AU2002336749A AU2002336749A1 (en) 2001-09-21 2002-09-19 Tricyclic indole derivatives as 5-ht ligands
JP2003528823A JP2005527477A (en) 2001-09-21 2002-09-19 Tricyclic indole derivatives as 5-HT ligands
EP02773527A EP1429776A2 (en) 2001-09-21 2002-09-19 Tricyclic indole derivatives as 5-ht ligands
MXPA04002615A MXPA04002615A (en) 2001-09-21 2002-09-19 Therapeutic 5-ht ligand compounds.
CA002460126A CA2460126A1 (en) 2001-09-21 2002-09-19 Tricyclic indole derivatives as 5-ht ligands
BRPI0212676-1A BR0212676A (en) 2001-09-21 2002-09-19 5-ht ligand therapeutic compounds, pharmaceutical compositions comprising such compounds and their uses

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32366601P 2001-09-21 2001-09-21
US60/323,666 2001-09-21

Publications (2)

Publication Number Publication Date
WO2003024976A2 WO2003024976A2 (en) 2003-03-27
WO2003024976A3 true WO2003024976A3 (en) 2004-02-12

Family

ID=23260193

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2002/030089 WO2003024976A2 (en) 2001-09-21 2002-09-19 Tricyclic indole derivatives as 5-ht ligands

Country Status (8)

Country Link
US (1) US6887868B2 (en)
EP (1) EP1429776A2 (en)
JP (1) JP2005527477A (en)
AU (1) AU2002336749A1 (en)
BR (1) BR0212676A (en)
CA (1) CA2460126A1 (en)
MX (1) MXPA04002615A (en)
WO (1) WO2003024976A2 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CL2004000826A1 (en) 2003-04-25 2005-03-04 Pfizer USE OF AN AGONIST FOR THE 5-HT2C RECEPTOR TO PREPARE A USEFUL MEDICINAL PRODUCT IN THE TREATMENT OF URINARY INCONTINENCE CAUSED BY STRESS, WITH THE CONDITION THAT THE AGONIST IS NOT 1- [6-CHLORINE-5- (TRIFLUOROMETIL) -2- PIRIDINIL] PIPERAZINA (ORG-129
WO2006022420A1 (en) 2004-08-25 2006-03-02 Takeda Pharmaceutical Company Limited Preventives/remedies for stress urinary incontinence and method of screening the same
AR059356A1 (en) * 2006-02-14 2008-03-26 Astrazeneca Ab NEW RADIOLIGANDS
EP2742936A1 (en) 2006-05-16 2014-06-18 Takeda Pharmaceutical Company Limited Fused heterocyclic compound and use thereof
US20100266504A1 (en) 2007-11-15 2010-10-21 Takahiro Matsumoto Condensed pyridine derivative and use thereof
WO2011071136A1 (en) 2009-12-11 2011-06-16 アステラス製薬株式会社 Therapeutic agent for fibromyalgia
US9216998B2 (en) * 2012-02-15 2015-12-22 Janssen Pharmaceutica Nv Tricyclic indole derivatives useful endothelial lipase inhibitors
JP7065951B2 (en) * 2017-09-22 2022-05-12 ジュビラント エピパッド エルエルシー Heterocyclic compound as a PAD inhibitor
CA3076476A1 (en) 2017-10-18 2019-04-25 Jubilant Epipad LLC Imidazo-pyridine compounds as pad inhibitors
CA3080677A1 (en) 2017-11-06 2019-05-09 Jubilant Prodel LLC Pyrimidine derivatives as inhibitors of pd1/pd-l1 activation
MX2020005363A (en) 2017-11-24 2020-10-01 Jubilant Episcribe Llc Heterocyclic compounds as prmt5 inhibitors.
US20210052600A1 (en) 2017-12-27 2021-02-25 Takeda Pharmaceutical Company Limited Therapeutic agents for stress urinary incontinence and incotinence of feces
MX2020009517A (en) 2018-03-13 2021-01-20 Jubilant Prodel LLC Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation.

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2330719A1 (en) * 1972-06-19 1974-01-10 Endo Lab PYRIDOPYRROLBENZOHETEROCYCLENE
US4219550A (en) * 1978-11-09 1980-08-26 E. I. Du Pont De Nemours And Company Cis- and trans- octahydropyridopyrrolobenzheterocycles
EP0322016A1 (en) * 1987-12-10 1989-06-28 Duphar International Research B.V 1,7-Annelated indolecarboxylic acid esters and -amides
EP0393766A2 (en) * 1989-04-18 1990-10-24 Duphar International Research B.V New 3-N substituted carbamoyl-indole derivatives
EP0403261A2 (en) * 1989-06-14 1990-12-19 Glaxo Group Limited Amide derivatives
EP0473550A1 (en) * 1990-08-27 1992-03-04 Sandoz Ltd. Indolonaphthyridines
WO2000006564A1 (en) * 1998-07-30 2000-02-10 Japan Tobacco Inc. Disubstituted maleimide compounds and medicinal utilization thereof
WO2000064899A1 (en) * 1999-04-23 2000-11-02 Pharmacia & Upjohn Company Tetracyclic azepinoindole compounds as 5-ht receptor ligands
WO2000077010A2 (en) * 1999-06-15 2000-12-21 Du Pont Pharmaceuticals Company Substituted heterocycle fused gamma-carbolines

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4938949A (en) 1988-09-12 1990-07-03 University Of New York Treatment of damaged bone marrow and dosage units therefor

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2330719A1 (en) * 1972-06-19 1974-01-10 Endo Lab PYRIDOPYRROLBENZOHETEROCYCLENE
US4219550A (en) * 1978-11-09 1980-08-26 E. I. Du Pont De Nemours And Company Cis- and trans- octahydropyridopyrrolobenzheterocycles
EP0322016A1 (en) * 1987-12-10 1989-06-28 Duphar International Research B.V 1,7-Annelated indolecarboxylic acid esters and -amides
EP0393766A2 (en) * 1989-04-18 1990-10-24 Duphar International Research B.V New 3-N substituted carbamoyl-indole derivatives
EP0403261A2 (en) * 1989-06-14 1990-12-19 Glaxo Group Limited Amide derivatives
EP0473550A1 (en) * 1990-08-27 1992-03-04 Sandoz Ltd. Indolonaphthyridines
WO2000006564A1 (en) * 1998-07-30 2000-02-10 Japan Tobacco Inc. Disubstituted maleimide compounds and medicinal utilization thereof
WO2000064899A1 (en) * 1999-04-23 2000-11-02 Pharmacia & Upjohn Company Tetracyclic azepinoindole compounds as 5-ht receptor ligands
WO2000077010A2 (en) * 1999-06-15 2000-12-21 Du Pont Pharmaceuticals Company Substituted heterocycle fused gamma-carbolines

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
J. NOZULAK ET AL.: "(+)-cis-4,5,7a,8,9,10,11,11a-Octahydro-7H-10-methylindolo[1,7-bc][2,6]naphthyridine: a 5-HT(2C/2B) receptor antagonist with low 5-HT(2A) receptor affinity", J. MED. CHEM., vol. 38, no. 1, 1995, pages 28 - 33, XP002215658 *
J. W. BLOWERS ET AL.: "Total Synthesis of Heptacyclic Aspidosperma Alkaloids. Part 1. Preliminary Experiments", J. CHEM. SOC., PERKIN TRANS. I, no. 9, 1987, pages 2079 - 2090, XP009002099 *
R. A. GLENNON ET AL.: "5-HT(6) serotonin receptor binding of indolealkylamines: a preliminary structure-affinity investigation", MED. CHEM. RES., vol. 9, no. 2, 1999, pages 108 - 117, XP001106724 *

Also Published As

Publication number Publication date
US6887868B2 (en) 2005-05-03
MXPA04002615A (en) 2004-07-08
EP1429776A2 (en) 2004-06-23
BR0212676A (en) 2006-05-23
CA2460126A1 (en) 2003-03-27
US20030087883A1 (en) 2003-05-08
WO2003024976A2 (en) 2003-03-27
JP2005527477A (en) 2005-09-15
AU2002336749A1 (en) 2003-04-01

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